Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5272576 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
Aromatic amines can be employed in the Bargellini reaction to generate useful intermediates. Rapid, practical access to functionalised, privileged structures may have significant utility in the synthesis of drug-like molecules. An improved synthesis of carfentanil analogues illustrates this point.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ken J. Butcher, Jenny Hurst,